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Dexmedetomidinine in the Prevention of Postoperative Delirium in the Intensive Care Unit After Cardiac Surgery
RECRUITINGPhase 3Sponsored by University of Novi Sad
Actively Recruiting
PhasePhase 3
SponsorUniversity of Novi Sad
Started2022-03-01
Est. completion2025-02
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT05849597
Summary
This is a prospective, randomized, single blinded, controlled clinical trial designed to compare the clinical effects of sedation with dexmedetomidine versus propofol in patients undergoing cardiac surgery.
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: * patients undergoing open heart surgery with the use of cardiopulmonary bypass (including coronary artery bypass grafting, valve repair/replacement, and combined) * left ventricular ejection fraction (LVEF) \>40%. Exclusion Criteria: * preoperative atrial fibrillation * previous history of interventionally treated arrhythmias * second and third degree atrioventricular block * bradycardia with heart rate ≤50/min * pacemaker * renal or hepatic insufficiency * emergency procedures * history of serious mental illness, delirium, and severe dementia
Conditions2
Heart DiseaseIntensive Care Unit Delirium
Interventions2
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Actively Recruiting
PhasePhase 3
SponsorUniversity of Novi Sad
Started2022-03-01
Est. completion2025-02
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT05849597